Pralidoxime Iodide Injection
- Packing: 20 Ml Ampoule.
- Available Strength : 25 Mg/Ml
Description
Product Description: Pralidoxime Iodide Injection is a meticulously formulated pharmaceutical solution designed to counteract the toxic effects of organophosphate poisoning. It contains pralidoxime iodide, a cholinesterase reactivator that restores the activity of acetylcholinesterase, which is inhibited by organophosphate compounds. Manufactured to the highest quality standards, this injection offers rapid and effective treatment for organophosphate toxicity.
Indications and Usage: Pralidoxime Iodide Injection is indicated for the treatment of poisoning due to organophosphate insecticides and nerve agents, such as sarin and soman. It is particularly useful in situations where prompt administration is crucial to prevent or reverse the toxic effects of these compounds on the nervous system.
Dosage and Administration: The dosage of Pralidoxime Iodide Injection varies depending on the severity of poisoning and the patient's age and weight. It is typically administered via intravenous infusion or intramuscular injection under the supervision of a qualified healthcare professional. The dosage regimen may involve initial bolus doses followed by continuous infusion or intermittent injections, as determined by the treating physician.
Dosage Forms and Strengths: Pralidoxime Iodide Injection is available as a sterile solution in vials containing specific concentrations of pralidoxime iodide formulated for parenteral administration. Each vial is carefully manufactured to ensure accurate dosing and optimal therapeutic outcomes.
Contraindications: This product is contraindicated in patients with a known hypersensitivity to pralidoxime iodide or any of the excipients. It should not be used in patients with carbamate insecticide poisoning or in those with irreversible cholinesterase inhibition. Additionally, it is contraindicated in patients with severe cardiovascular disease or hypertension.
Warnings and Precautions: Healthcare providers should exercise caution when prescribing Pralidoxime Iodide Injection to patients with a history of allergic reactions or renal impairment. Rarely, serious adverse effects such as hypersensitivity reactions, tachycardia, and hypertension may occur. Patients should be monitored closely for signs of these adverse effects during therapy.
Adverse Reactions/Side Effects: Common adverse reactions associated with Pralidoxime Iodide Injection include local irritation at the injection site, dizziness, and headache. Rarely, serious adverse effects such as anaphylaxis, cardiac arrhythmias, and respiratory depression may occur. Patients should be advised to report any unusual symptoms promptly.
Drug Interactions: Concomitant use of Pralidoxime Iodide Injection with other cholinesterase inhibitors or drugs that prolong the QT interval may increase the risk of adverse effects or alter the pharmacokinetics of pralidoxime. Healthcare providers should review the patient's medication profile carefully to avoid potential drug interactions.
Use In Specific Populations Description: Safety and efficacy of Pralidoxime Iodide Injection in pediatric patients, pregnant women, and nursing mothers have not been established conclusively. Healthcare providers should assess the potential risks and benefits before prescribing this medication in these populations.
How Supplied/Storage and Handling: Pralidoxime Iodide Injection is supplied as a sterile solution in vials for parenteral administration. It should be stored at controlled room temperature away from light and moisture. Care should be taken to avoid freezing or excessive heat exposure. Unused portions should be discarded according to standard procedures for biohazardous waste.